Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Acetic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NOS3 known ✓ | P29474 | 2/20 | 0.30 |
| ▸ | NOS1 known ✓ | P29475 | 2/20 | 0.30 |
| ▸ | NOS2 known ✓ | P35228 | 2/20 | 0.30 |
| ▸ | CNR1 | P21554 | 1/20 | 0.33 |
| ▸ | CNR2 | P34972 | 1/20 | 0.33 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.30 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.30 |
| ▸ | TSHR | P16473 | 1/20 | 0.30 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL6551938 | 0.85 | — | — | |
| Acetic Acid SCHEMBL452674 | 0.82 | CNR1 (0.33) | CNR1CNR2NOS3NOS1NOS2 | |
| SCHEMBL7615127 | 0.72 | GPR84 (0.36) | TSHR | |
| SCHEMBL28789890 | 0.72 | CNR1 (0.40) | CNR1CNR2TSHR | |
| SCHEMBL7928645 | 0.71 | FOLH1 (0.41) | CYP1A2CYP3A4TSHR | |
| SCHEMBL8370840 | 0.71 | CNR1 (0.35) | CNR1CNR2 | |
| Bicarbonate SCHEMBL4532520 | 0.68 | CNR1 (0.33) | CNR1CNR2 | |
| SCHEMBL29105368 | 0.67 | TSHR (0.40) | CNR1CNR2TSHR | |
| SCHEMBL11693016 | 0.67 | TBXAS1 (0.43) | NOS3NOS1NOS2CYP1A2CYP3A4 | |
| SCHEMBL7920483 | 0.67 | SLC22A6 (0.38) | TSHR |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 55 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0862589-B1 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | SUMITOMO BAKELITE CO (JP) | 2004-02-18 | — | — | EP | claimed |
| US-20020128408-A1 | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | INTERNATIONAL BUSINESS MACHINES CORPORATION | 2002-09-12 | — | — | US | claimed |
| EP-0828768-B1 | HOMOPOLYMERS AND COPOLYMERS OF CATIONICALLY POLYMERIZABLE MONOMERS AND METHOD OF THEIR PREPARATION | GOODRICH CO B F (US) | 2001-04-18 | — | — | EP | claimed |
| CN-1269810-A | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | GOODRICH CO B F (US) | 2000-10-11 | — | — | CN | claimed |
| EP-1021477-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 2000-07-26 | — | — | EP | claimed |
| US-6031058-A | POLYMERS OF THE INVENTION INCLUDE POLYCYCLIC REPEAT UNITS THAT CONTAIN PENDANT SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 2000-02-29 | — | — | US | claimed |
| WO-1999014256-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 1999-03-25 | — | — | WO | claimed |
| EP-0729480-B1 | ADDITION POLYMERS DERIVED FROM NORBORNENE-FUNCTIONAL MONOMERS AND PROCESS THEREFOR | GOODRICH CO B F (US) | 1999-01-27 | — | — | EP | claimed |
| EP-0862589-A2 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 1998-09-09 | — | — | EP | claimed |
| CN-1185164-A | Homopolymers and copolymers of cationically polymerizable monomers, and prepn. method therefor | GOODRICH CO B F (US) | 1998-06-17 | — | — | CN | claimed |
| US-5741869-A | REACTION MIXTURE FOR FORMING ADDITION POLYMER COMPRISING NORBORNENE-FUNCTIONAL MONOMER, SOLVENT, GROUP 8 METAL-CONTAINING CATALYST SYSTEM, CHAIN TRANSFER AGENT | THE B.F. GOODRICH COMPANY (US) | 1998-04-21 | — | — | US | claimed |
| EP-0828768-A1 | HOMOPOLYMERS AND COPOLYMERS OF CATIONICALLY POLYMERIZABLE MONOMERS AND METHOD OF THEIR PREPARATION | The B.F. Goodrich Company (US) | 1998-03-18 | — | — | EP | claimed |
| WO-1997020871-A2 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 1997-06-12 | — | — | WO | claimed |
| EP-0758657-A2 | Addition polymers derived from norbornene-functional monomers and process therefor | The B.F. Goodrich Company (US) | 1997-02-19 | — | — | EP | claimed |
| WO-1996037529-A1 | HOMOPOLYMERS AND COPOLYMERS OF CATIONICALLY POLYMERIZABLE MONOMERS AND METHOD OF THEIR PREPARATION | THE B.F. GOODRICH COMPANY (US) | 1996-11-28 | — | — | WO | claimed |
| US-5571881-A | Addition polymers derived from norbornene-functional monomers and process therefor | THE B. F. GOODRICH COMPANY (US) | 1996-11-05 | — | — | US | claimed |
| EP-0729480-A1 | ADDITION POLYMERS DERIVED FROM NORBORNENE-FUNCTIONAL MONOMERS AND PROCESS THEREFOR | The B.F. Goodrich Company (US) | 1996-09-04 | — | — | EP | claimed |
| WO-1995014048-A9 | ADDITION POLYMERS DERIVED FROM NORBORNENE-FUNCTIONAL MONOMERS AND PROCESS THEREFOR | — | 1995-07-27 | — | — | WO | claimed |
| WO-1995014048-A1 | ADDITION POLYMERS DERIVED FROM NORBORNENE-FUNCTIONAL MONOMERS AND PROCESS THEREFOR | THE B.F. GOODRICH COMPANY (US) | 1995-05-26 | — | — | WO | claimed |
| EP-0885405-B1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | SUMITOMO BAKELITE CO (JP) | 2005-06-08 | — | — | EP | disclosed |
| CN-1198181-C | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | SUMITOMO BAKELITE CO (JP) | 2005-04-20 | — | — | CN | disclosed |
| US-6790579-B1 | PHOTOACID INITIATOR GENERATES ACID EFFECTING POLARITY CHANGE RENDERING POLYMER WATER SOLUBLE IN AREAS EXPOSED TO IMAGING SOURCE; INTEGRATED CIRCUITS, SEMICONDUCTORS | SUMITOMO BAKELITE CO., LTD. (JP) | 2004-09-14 | — | — | US | disclosed |
| US-6723486-B2 | POLYMERIZING AT LEAST TWO TYPES OF POLYCYCLIC (NORBORNENE) MONOMERS ONE OF WHICH CONTAINING A PENDANT ACID LABILE GROUP AND ANOTHER OF WHICH CONTAINING A PENDNT POLAR FUNCTIONAL GROUP USING A GROUP 8 TRANSITION METAL CATALYST | SUMITOMO BAKELITE CO., LTD. (JP) | 2004-04-20 | — | — | US | disclosed |
| EP-0862589-B1 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | SUMITOMO BAKELITE CO (JP) | 2004-02-18 | — | — | EP | disclosed |
| EP-1157058-B1 | METHOD OF PREPARING NORBORNENE SULFONAMIDE POLYMERS | SUMITOMO BAKELITE CO (JP) | 2003-06-25 | — | — | EP | disclosed |
| US-20020136982-A1 | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | THE B.F. GOODRICH COMPANY | 2002-09-26 | — | — | US | disclosed |
| US-20020128408-A1 | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | INTERNATIONAL BUSINESS MACHINES CORPORATION | 2002-09-12 | — | — | US | disclosed |
| US-6426396-B2 | PARAPHENYLENE POLYMER PRODUCED BY REMOVING THE SUBSTITIUENTS FROM THE CYCLOHEXADIENE RING; NICKEL BASED CATALYST; ELECTROCONDUCTIVITY | KABUSHIKI KAISHA TOYOTA CHUO KENKYUSHO (JP) | 2002-07-30 | — | — | US | disclosed |
| US-6420503-B1 | POLYCARBONS/OTHER/ | SUMITOMO BAKELITE CO. LTD. (JP) | 2002-07-16 | — | — | US | disclosed |
| US-20020007026-A1 | POLY (CYCLIC CONJUGATED DIENE) AND PROCESS FOR PRODUCING THE SAME | NAKANO MITSURU (JP) | 2002-01-17 | — | — | US | disclosed |
| EP-1157058-A1 | METHOD OF PREPARING NORBORNENE SULFONAMIDE POLYMERS | The B.F. Goodrich Company (US) | 2001-11-28 | — | — | EP | disclosed |
| US-6235849-B1 | INCLUDE COPOLYMERS WITH ONE OR MORE COMONOMERS SUCH AS NORBORNENE, ETHYLENE, AN ACRYLATE OR SULFUR DIOXIDE OR CARBON MONOXIDE; ALSO RING-OPENING METATHESIS POLYMERIZATION; GROUP VIII METAL COMPOUND CATALYST | THE B. F. GOODRICH COMPANY | 2001-05-22 | — | — | US | disclosed |
| US-6232417-B1 | USING COORDINATION CATALYST | THE B. F. GOODRICH COMPANY | 2001-05-15 | — | — | US | disclosed |
| EP-0828768-B1 | HOMOPOLYMERS AND COPOLYMERS OF CATIONICALLY POLYMERIZABLE MONOMERS AND METHOD OF THEIR PREPARATION | GOODRICH CO B F (US) | 2001-04-18 | — | — | EP | disclosed |
| US-6136499-A | RADIATION SENSITIVE PHOTORESIST COMPOSITION COMPRISING A PHOTOACID INITIATOR AND A POLYCYCLIC POLYMER COMPRISING REPEATING UNITS THAT CONTAIN PENDANT ACID LABILE GROUPS | THE B. F. GOODRICH COMPANY (US) | 2000-10-24 | — | — | US | disclosed |
| CN-1269810-A | Photoresist compositions comprising polycyclic polymers with acid labile pendant groups | GOODRICH CO B F (US) | 2000-10-11 | — | — | CN | disclosed |
| WO-2000046268-A1 | NORBORNENE SULFONAMIDE POLYMERS | THE B.F. GOODRICH COMPANY (US) | 2000-08-10 | — | — | WO | disclosed |
| WO-2000046267-A1 | METHOD OF PREPARING NORBORNENE SULFONAMIDE POLYMERS | THE B.F. GOODRICH COMPANY (US) | 2000-08-10 | — | — | WO | disclosed |
| EP-1021477-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 2000-07-26 | — | — | EP | disclosed |
| EP-1021750-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 2000-07-26 | — | — | EP | disclosed |
| US-6031058-A | POLYMERS OF THE INVENTION INCLUDE POLYCYCLIC REPEAT UNITS THAT CONTAIN PENDANT SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 2000-02-29 | — | — | US | disclosed |
| US-5912313-A | MOLDINGS, COATINGS, ADHESIVES, MEMBRANES; OXIDATION, HEAT AND CHEMICAL RESISTANCE; DIELECTRICS, INTEGRATED CIRCUITS | THE B. F. GOODRICH COMPANY (US) | 1999-06-15 | — | — | US | disclosed |
| WO-1999014635-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 1999-03-25 | — | — | WO | disclosed |
| WO-1999014256-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 1999-03-25 | — | — | WO | disclosed |
| EP-0758657-B1 | Addition polymers derived from norbornene-functional monomers | GOODRICH CO B F (US) | 1999-02-03 | — | — | EP | disclosed |
| EP-0729480-B1 | ADDITION POLYMERS DERIVED FROM NORBORNENE-FUNCTIONAL MONOMERS AND PROCESS THEREFOR | GOODRICH CO B F (US) | 1999-01-27 | — | — | EP | disclosed |
| EP-0885405-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 1998-12-23 | — | — | EP | disclosed |
| EP-0862589-A2 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 1998-09-09 | — | — | EP | disclosed |
| US-5741869-A | REACTION MIXTURE FOR FORMING ADDITION POLYMER COMPRISING NORBORNENE-FUNCTIONAL MONOMER, SOLVENT, GROUP 8 METAL-CONTAINING CATALYST SYSTEM, CHAIN TRANSFER AGENT | THE B.F. GOODRICH COMPANY (US) | 1998-04-21 | — | — | US | disclosed |
| US-5677405-A | COPOLYMER OF NORBORNENE-TYPE MONOMER WHICH UNDERGOES ADDITION POLYMERIZATION AND CATIONICALLY POLYMERIZABLE MONOMER | THE B.F. GOODRICH COMPANY (US) | 1997-10-14 | — | — | US | disclosed |
| WO-1997033198-A1 | PHOTORESIST COMPOSITIONS COMPRISING POLYCYCLIC POLYMERS WITH ACID LABILE PENDANT GROUPS | THE B.F. GOODRICH COMPANY (US) | 1997-09-12 | — | — | WO | disclosed |
| WO-1997020871-A2 | ADDITION POLYMERS OF POLYCYCLOOLEFINS CONTAINING SILYL FUNCTIONAL GROUPS | THE B.F. GOODRICH COMPANY (US) | 1997-06-12 | — | — | WO | disclosed |
| EP-0758657-A2 | Addition polymers derived from norbornene-functional monomers and process therefor | The B.F. Goodrich Company (US) | 1997-02-19 | — | — | EP | disclosed |
| US-5571881-A | Addition polymers derived from norbornene-functional monomers and process therefor | THE B. F. GOODRICH COMPANY (US) | 1996-11-05 | — | — | US | disclosed |
| US-5569730-A | HAVING TERMINAL END GROUP DERIVED FROM CHAIN TRANSFER AGENT CONTAINING TERMINAL OLEFINIC DOUBLE BOND | THE B. F. GOODRICH COMPANY (US) | 1996-10-29 | — | — | US | disclosed |
| US-5569730-A | HAVING TERMINAL END GROUP DERIVED FROM CHAIN TRANSFER AGENT CONTAINING TERMINAL OLEFINIC DOUBLE BOND | THE B. F. GOODRICH COMPANY (US) | 1996-10-29 | — | — | US | disclosed |